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  • C07C275/46—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups containing any of the groups, X being a hetero atom, Y being any atom, e.g. acylureas
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  • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
  • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
  • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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  • C07C271/06—Esters of carbamic acids
  • C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
  • C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
  • C07C271/22—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by carboxyl groups
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  • C07C275/46—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups containing any of the groups, X being a hetero atom, Y being any atom, e.g. acylureas
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  • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
  • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
  • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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  • C07D277/04—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
  • C07D277/06—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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  • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
  • C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
  • C07D295/20—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
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• • C—CHEMISTRY; METALLURGY
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  • C07K—PEPTIDES
  • C07K11/00—Depsipeptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof

Definitions

• Endoparasiticidal compositions based on didepsipeptides, new didepsipeptides and processes for their production The present invention relates to the use of didepsipeptides for combating endoparasites, new didepsipeptides and processes for their production.
• didepsipeptides are used as starting materials for endoparasiticidal cyclic depsipeptides (cf. total synthesis of PF 1022 A: JP Pat. 05 229 997; Makoto Ohyama et al., Biosci. Biotech. Biochem. 58 (6), 1994, p. 1193- 1194;
• R 1 represents hydrogen, straight-chain or branched alkyl, cycloalkyl.
• R 1 and R 2 together with the atoms to which they are attached represent a 5- or 6-membered ring which may be replaced by oxygen, Sulfur, sulfoxyl or sulfonyl can be interrupted and optionally substituted,
• R 2 and R 3 independently of one another are hydrogen, straight-chain or branched alkyl, alkenyl, cycloalkyl, cycloalkylalkyl, aryl,
• R 2 and R 3 together represent a spirocyclic ring which is optionally substituted
• R 4 and R 3 independently of one another represent hydrogen, straight-chain or branched alkyl, alkenyl, cycloalkyl, cycloalkylalkyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, which are optionally substituted are, or
• R 4 and R 3 together represent a spirocyclic ring which is optionally substituted
• R 6 represents hydrogen, hydroxy, alkoxy, alkylcarbonyl, haloalkylcarbonyl, alkylsulfonyl, nitro or cyan
• R 7 represents hydrogen or alkyl
• Q represents straight-chain or branched alkyl, alkenyl, alkynyl, cycloalkyl, aryl, arylalkyl, hetaryl or hetarylalkyl, which are optionally substituted, or if appropriate for a radical from the group G 2 and G 3 ,
• Y stands for oxygen, sulfur or -NR 9 , R 8 for the case that Y stands for nitrogen, one above
• Nitrogen atom-linked cyclic amino group can mean
• R 8 and R 9 independently of one another represent hydrogen, straight-chain or branched alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, aryl, arylalkyl, hetaryl, hetarylalkyl, which are optionally substituted, or
• R 8 and R 9 together with the adjacent N atom for a carbocyclic 5-, 6- or 7-membered ring system or for a 7 to 10-membered bicyclic ring system which may also be replaced by oxygen, sulfur, sulfoxyl,
• Sulfonyl, carbonyl, -NO-, -N , -NR 11 - or can be interrupted by quaternized nitrogen and is optionally substituted, R 10 represents hydrogen or alkyl,
• R 11 represents hydrogen, straight-chain or branched alkyl
• R 12 and R 13 independently of one another are hydrogen, straight-chain or branched alkyl, alkylcarbonyl, alkylsulfonyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, aryl,
• Arylcarbonyl, arylsulfonyl, arylalkyl, hetaryl, hetaryl carbonyl, hetarylsulfonyl or hetarylalkyl, which are optionally substituted, are or
• R 14 represents hydrogen, straight-chain or branched alkyl, cycloalkyl, arylalkyl or hetarylalkyl, which are optionally substituted
• R 15 and R 16 independently of one another are hydrogen, straight-chain or branched alkyl, alkylcarbonyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, arylalkyl or hetarylalkyl, which are optionally substituted
• R 15 and R 16 together with the adjacent NO group mean a carbocyclic 5-, 6- or 7-membered rings, as well as their optical isomers and racemates, are used to combat endoparasites in medicine and veterinary medicine.
• R 1 represents hydrogen, straight-chain or branched alkyl having up to 6 carbon atoms, C 3-6 -cycloalkyl, aryl-C 1-2 alkyl, or Het-C 1-2 -alkyl, which are optionally substituted, stand,
• R 1 and R 2 together with the atoms to which they are attached represent a 5- or 6-membered ring which can optionally be interrupted by sulfur and is optionally substituted,
• R 2 and R 3 independently of one another are hydrogen, straight-chain or branched alkyl having up to 6 carbon atoms, haloalkyl,
• Hydroxyalkyl C 1-4 alkanoyloxyalkyl, C 1-2 alkoxyalkyl, mercaptoalkyl, C 1-2 alkylthioalkyl, C 1-2 alkylsulfinylalkyl, C 1-2 alkylsulfonylalkyl, carboxyalkyl, carbamoylalkyl, aminoalkyl, C 1-6 - Alkylaminoalkyl, C 1-6 - dialkylaminoalkyl, guanidinoalkyl, which may optionally be substituted by one or two benzyloxycarbonyl residues or by one, two, three or four C 1-2 alkyl residues, C 1-4 alkoxycarbonylaminoalkyl, C 2-6 - Alkenyl, C 3-6 -cycloalkyl, C 3-6 -cycloalkyl-C 1 -2 -alkyl and optionally substituted aryl, aryl-C 1-2 -alkyl,
• R 6 represents hydrogen, hydroxy, C 1-4 alkoxy, C 1-4 alkylcarbonyl, C 1-4 - haloalkylcarbonyl, C 1-4 alkylsulfonyl, nitro or cyano
• R 7 represents hydrogen or C 1-4 alkyl
• Q for straight-chain or branched C 1-6 alkyl, C 1-6 haloalkyl, hydroxyC 1-6 alkyl, C 1-4 alkanoyloxy-C 1-6 alkyl, C 1-2 alkoxy-C 1-6 -alkyl, mercapto-C 1-6 -alkyl, C 1-2 -alkylthio-C 1-6 -alkyl, C 1-2 -alkylsulfinyl-C 1-6 -alkyl, C 1-2 - alkylsulfonyl-C 1-6 alkyl, carboxy C 1-6 - alkyl, carbamoyl-C 1-6 -alkyl, amino-C 1-6 alkyl, C 1-6 alkylamino C 1-6 alkyl, C 1-6 dialkylaminoalkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 2-6 - haloalkenyl, C 3-6 -Cycoalkyl, and represents
• Y stands for oxygen, sulfur or -NR 9 , R 8 for the case that Y stands for nitrogen, one above
• Nitrogen atom-linked cyclic amino group can mean
• R 8 and R 9 independently of one another are hydrogen, straight-chain or branched C 1-6 alkyl, C 1-6 alkenyl, C 1-6 alkynyl, C 3-6 cycloalkyl, C 3-6 cycloalkyl-C 1 -2- alkyl, aryl, arylalkyl,
• R 10 represents hydrogen or C 1-4 alkyl
• R 11 is hydrogen, straight-chain or branched C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-8 cycloalkyl, C 3-8 cycloalkylC 1-2 alkyl, C 1-4 alkoxy carbonyl, C 1-4 alkylcarbonyl, C 3-6 cycloalkylcarbonyl, cyano, aryl, arylC 1-2 alkyl, hetaryl, hetarylC 1-2 alkyl, which are optionally substituted are, and represents hydroxy, C 1-6 alkoxy, C 2-6 alkenyloxy, C 2-6 alkynyloxy, C 3-7 cycloalkyloxy, C 3-7 cycloalkylalkyloxy, aryloxy, aryl-C 1 -2 -alkyloxy, hetaryloxy, hetaryl-C 1-2 -alkyloxy, which are optionally substituted, is, or the radicals -NR
• R 12 and R 13 are independently hydrogen, straight or branched C 1-6 - alkyl, C 1-6 - alkyl carbonyl, C 1-6 alkylsulfonyl,
• R 14 represents hydrogen, straight-chain or branched C 1-6 -al
• R 15 and R 16 independently of one another are hydrogen, straight-chain or branched C 1-6 alkyl, C 1-6 alkylcarbonyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 3- 6 -cycloalkyl-C 1-2 -alkyl, allyl-C 1-2 -alkyl or hetaryl-C 1-2 -alkyl, which are optionally substituted, mean
• R 15 and R 16 together with the adjacent NO group represent a carbocyclic 5-, 6- or 7-membered ring, and their optical isomers and racemates, for combating endoparasites in medicine and veterinary medicine.
• R 1 represents hydrogen, straight-chain or branched C 1-4 alkyl, C 3-6 cycloalkyl, aryl C 1-2 alkyl or hetaryl C 1 -2 alkyl, which are optionally substituted, and
• R 1 and R 2 together with the atoms to which they are attached represent a 5- or 6-membered ring which may be replaced by oxygen, Sulfur, sulfoxyl or sulfonyl can be interrupted and optionally substituted, R 2 for hydrogen, straight-chain or branched alkyl with up to 6
• R 3 and R 4 represent hydrogen
• R represents hydrogen, straight-chain or branched alkyl having up to 6 carbon atoms, alkenyl having up to 4 carbon atoms, C 3-6 cycloalkyl, C 3-6 cycloalkyl-C 1-2 -alkyl, aryl, aryl-C 1-2 alkyl, hetaryl, hetaryl-C 1-2 -alkyl which are optionally substituted,
• R 6 represents hydrogen, hydroxy, C 1-4 alkoxy, C 1-4 alkylcarbonyl, C 1-4 haloalkylcarbonyl, C 1-4 alkylsulfonyI, nitro or cyano, and
• R 7 represents hydrogen or C 1-4 alkyl
• Q represents straight-chain or branched C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl or hetaryl-C 1-2 -alkyl, which are optionally substituted, or optionally for a radical from the group G 2 and G 3 , wherein
• Y represents oxygen, sulfur or -NR 9 ,
• R 8 when Y is nitrogen, can mean a cyclic amino group linked via a nitrogen atom
• R 8 and R 9 independently of one another represent hydrogen, straight or branched C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3- 6 cycloalkyl, C 3-3 -cycloalkyl-C 1 -2- alkyl, hetaryl or hetaryl -C 1-2 alkyl, which are optionally substituted, or
• R 8 and R 9 together with the adjacent N atom represent a carbocyclic 5-, 6- or 7-membered ring system or a 7 to 10-membered bicyclic ring system which may also be replaced by oxygen, sulfur, sulfoxyl,
• Sulfonyl, carbonyl, -NO-, -N , -NR 1 1 - or can be interrupted by quaternized nitrogen and is optionally substituted,
• R 10 represents hydrogen or C 1-4 alkyl
• R 11 represents hydrogen, straight-chain or branched C 1-6 alkyl
• R 14 represents hydrogen, straight-chain or branched C 1-6 alkyl,
• R 15 and R 16 are independently hydrogen, straight or branched C 1-6 alkyl, C 1 -6 alkylcarbonyl, C 2-6 - alkenyl, C 2-6 alkynyl, or C 3-6 -Cycl oal kyl, di e are optionally substituted, mean, and
• G 2 stands for tert-butyloxy, benzyloxy and 4-nitro-benzyloxy
• radical B stands for radicals other than tert-butyloxy, benzyloxy and 4-nitro-benzyloxy, and their optical isomers and racemates.
• radicals R 1 , R 2 , R 3 , G, Q, and X have the meaning given under point 2, or their carboxyactivated fourth derivatives or their alkali metal salts, if appropriate in the presence of a catalyst, if appropriate in the presence of an acid binder and optionally in the presence of a diluent, with
• radicals R 4 , R 3 and B have the meaning given under point 2 and Z represents a suitable leaving group, for example halogen such as bromine, chlorine fluorine or hydroxyl, or b) N-terminally deblocked didepsipeptides of the general formula ( Ib)
• radicals R 1 , R 2 , R 3 , R 4 , R 5 and B have the meaning given under point 2, optionally in the presence of a catalyst, optionally in the presence of an acid binder and optionally in the presence of a diluent, with compounds of the general formula ( IV) in which the radicals G, Q, W and X have the meaning given under point 2 and W represents a suitable leaving group, such as halogen, alkoxy, alkylthio or aryloxy, or c) N-terminally deblocked didepsipeptides of the general formula (Ib )
• radicals R 1 , R 2 , R 3 , R 4 , R 5 and B have the meaning given under point 2, optionally in the presence of a catalyst, optionally in the presence of an acid binder and optionally in the presence of a diluent, with compounds of the general Formulas (V) or (VI) in which the radicals R 8 , G 1 , X, X 1 and Y have the meaning given under point 2, or to represent the depsipeptides of the general formula (Ia) and their salts in which the group represents carboxy and Y represents oxygen,
• M represents a monovalent alkali metal cation, preferably lithium, sodium, potassium or cesium, in particular potassium or cesium, then in a second reaction step the resulting alkali metal salt of the formula (VIII)
• M stands for a salt-like metal cation equivalent, with alkylating agents of formula (IX) in which R 8 has the meaning given under point 2 and Hal represents a halogen such as fluorine, chlorine, bromine or iodine, if appropriate in the presence of a diluent and if appropriate in the presence of a basic reaction auxiliary, or e) didepsipeptides of the general formula (Ic)
• Formula (I) provides a general definition of the substituted didepsipeptides and their salts according to the invention.
• the substituted didepsipeptides according to the invention of the formula (I) and their acid addition salts and metal salt complexes have very good endoparasiticidal, in particular anthelmintic, effects and can preferably be in the range of
• Veterinary medicine can be used.
• Optionally substituted alkyl alone or as part of a radical in the general formulas means straight-chain or branched alkyl having preferably 1 to 6, in particular 1 to 4, carbon atoms. Examples include optionally substituted methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-
• Methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl and tert-butyl may preferably be mentioned.
• Optionally substituted alkenyl alone or as part of a radical in the general formulas means straight-chain or branched alkenyl with preferably 1 to 6, in particular 1 to 4, carbon atoms.
• Examples include optionally substituted vinyl, 2-propenyl, 2-butenyl, 3-butenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-methyl- 2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, 1,1- Dimethyl-2-propenyl, 1,2-dimethyl-2-propenyl, 1-ethyl-2-propenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, 1-methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-methyl-2-pentenyl, 4-methyl-2-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl, 1-methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl
• Optionally substituted alkynyl alone or as part of a radical in the general formulas means straight-chain or branched alkynyl having preferably 1 to 6, in particular 1 to 4, carbon atoms.
• Examples include optionally substituted ethynyl, 2-propynyl, 2-butynyl, 3-butynyl, 1-methyl-2-propynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1-methyl-3-butynyl, 2- Methyl-3-butynyl, 1-methyl-2-butynyl, 1,1-dimethyl-2-propynyl, 1-ethyl-2-propynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl, 1-methyl-2-pentynyl, 1-methyl-3-pentynyl, 1-methyl-4-pentynyl, 2-methyl-3-penty
• Optionally substituted cycloalkyl alone or as part of a radical in the general formulas means mono-, bi- and tricyclic cycloalkyl, preferably with 3 to 10, in particular with 3, 5 or 7 carbon atoms.
• Examples of optionally substituted cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, bicyclo [2.2.1] heptyl, bicyclo [2.2.2] octyl and adamantyl may be mentioned.
• Haloalkyl alone or as part of a radical in the general formulas contains 1 to 4, in particular 1 or 2, carbon atoms and preferably 1 to 9, in particular 1 to 5 identical or different halogen atoms, preferably fluorine, chlorine and bromine, in particular fluorine and chlorine.
• Examples include trifluoromethyl, trichloromethyl, chlorodifluoromethyl, dichlorofluoromethyl, chloromethyl, bromomethyl, 1-fluoroethyl, 2-fluoroethyl, 2, 2-difluoroethyl, 2,2,2-trifluoroethyl, 2,2,2-trichloroethyl, 2-chloro-2 , 2-difluoroethyl, pentafluoroethyl and pentafluoro-tert-butyl called.
• Optionally substituted alkoxy alone or as part of a radical in the general formulas means straight-chain or branched alkoxy with preferably 1 to 6, in particular 1 to 4, carbon atoms. Examples include optionally substituted methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy,
• Optionally substituted haloalkoxy alone or as part of a radical in the general formulas means straight-chain or branched haloalkoxy with preferably 1 to 6, in particular 1 to 4, carbon atoms.
• Examples include optionally substituted difluoromethoxy, trifluoromethoxy, trichloromethoxy, chlorodifluoromethoxy, 1-fluoroethoxy, 2-fluoroethoxy, 2,2-difluoroethoxy, 1,1,2,2, tetrafluoroethoxy, 2,2,2-trifluoroethoxy and 2-chloro - 1, 1,2-trifluoroethoxy called.
• Optionally substituted alkylthio alone or as part of a radical in the general formulas means straight-chain or branched alkylthio with preferably 1 to 6, in particular 1 to 4, carbon atoms.
• Examples of optionally substituted methylthio, ethylthio, n-propylthio, isopropylthio, n-butylthio, isobutylthio, sec-butylthio and tert-butylthio may be mentioned.
• Optionally substituted haloalkylthio alone or as part of a radical in the general formulas means straight-chain or branched haloalkylthio with preferably 1 to 6, in particular 1 to 4, carbon atoms.
• Examples include optionally substituted difluoromethylthio, tri fluoromethylthio, trichloromethylthio, chlorodifluoromethylthio, 1-fluoroethylthio, 2-fluoroethylthio, 2,2-di-fluoroethylthio, 1, 1, 2,2, -Tetrafluorethylthio, 2,2,2-trifluoroethylthio and 2-chloro-1,1,2 -trifluoroethylthio called.
• Optionally substituted alkylcarbonyl alone or as part of a radical in the general formulas means straight-chain or branched
• Alkylcarbonyl with preferably 1 to 6, in particular 1 to 4 carbon atoms.
• Examples of optionally substituted methylcarbonyl, ethylcarbonyl, n-propylcarbonyl, isopropylcarbonyl, n-butylcarbonyl, isobutylcarbonyl, sec-butylcarbonyl and tert-butylcarbonyl may be mentioned.
• Optionally substituted cycloalkylcarbonyl alone or as part of a radical in the general formulas means mono-, bi- and tricyclic cycloalkylcarbonyl, preferably with 3 to 10, in particular with 3, 5 or 7 carbon atoms.
• Examples include optionally substituted cyclopropylcarbonyl, cyclobutylcarbonyl, cyclopentylcarbonyl, cyclohexylcarbonyl, cycloheptylcarbonyl, cyclooctylcarbonyl, bicyclo [2.2.1] heptylcarbonyl,
• Bicyclo [2.2.2] called octylcarbonyl and adamantylcarbonyl.
• Optionally substituted alkoxycarbonyl alone or as part of a radical in the general formulas means straight-chain or branched alkoxycarbonyl with preferably 1 to 6, in particular 1 to 4, carbon atoms.
• Examples of optionally substituted methoxycarbonyl, ethoxycarbonyl, n-propoxycarbonyl, isopropoxycarbonyl, n-butoxycarbonyl, isobutoxycarbonyl, sec-butoxycarbonyl and tert-butoxycarbonyl may be mentioned.
• Aryl is, for example, a mono-, di- or polynuclear aromatic radical such as phenyl, naphthyl, tetrahydronaphthyl, indanyl, fluorenyl and the like, preferably phenyl or naphthyl.
• Optionally substituted aryl in the general formulas preferably means optionally substituted phenyl or naphthyl, especially phenyl.
• Optionally substituted arylalkyl in the general formulas preferably means optionally substituted arylalkyl in the aryl part and / or alkyl with preferably 6 or 10, in particular 8 carbon atoms in the aryl part
• phenyl or naphthyl, especially phenyl preferably 1 up to 4, in particular 1 or 2 carbon atoms in the alkyl part, where the alkyl part can be straight-chain or branched.
• Substituted benzyl and phenylethyl may be mentioned as examples and preferably.
• Optionally substituted hetaryl alone or as part of a radical in the general formulas means 5- to 7-membered rings with preferably 1 to
• heteroatoms in the heteroaromatics are oxygen, sulfur or nitrogen.
• the optionally substituted radicals of the general formulas can carry one or more, preferably 1 to 3, in particular 1 to 2 identical or different substituents.
• Examples of preferred substituents are:
• Alkyl groups such as methylamino, methylethylamino, dimethylamino, n-propylamino, isopropylamino, methyl-n-butylamino; Alkylcarbonyl radicals such as methylcarbonyl; Alkoxycarbonyl preferably having 2 to 4, in particular 2 to 3, carbon atoms, such as methoxycarbonyl and ethoxycarbonyl; Alkylsulfinyl with 1 to 4, in particular 1 to 2 carbon atoms; Halosulfinyl with 1 to 4, in particular 1 to 2 carbon atoms and 1 to 5 halogen atoms such as trifluoromethylsilfinyl; Sulfonyl (-SO 2 -OH); Alkylsulfonyl preferably having 1 to 4, in particular 1 or 2, carbon atoms, such as methylsulfonyl and ethylsulfonyl; Haloalkylsulfonyl having 1 to 4,
• Suitable cyclic amino groups are heteroaromatic or aliphatic ring systems with one or more nitrogen atoms as heteroatoms, in which the heterocycles can be saturated or unsaturated, one ring system or more condensed ring systems, and optionally contain further heteroatoms such as nitrogen, oxygen and sulfur, etc.
• cyclic amino groups can also mean a spiro ring or a bridged ring system.
• the number of atoms which form cyclic amino groups is not restricted, for example they consist of 3 to 8 atoms in the case of a single-ring system and 7 to 11 atoms in the case of a three-ring system.
• Examples of cyclic amino groups with saturated and unsaturated monocyclic groups with a nitrogen atom as hetero atom are 1-azetidinyl, pyrrolidino, 2-pyrrolin-1-yl, 1-pyrrolyl, piperidino, 1,4-dihydropyridin-1-yl, 1,2, 5,6-tetrahydropyridin-1-yl called homopiperidino;
• Examples of cyclic amino groups with saturated and unsaturated monocyclic groups with two or more nitrogen atoms as heteroatoms are 1- imidazolidinyl, 1-imidazolyl, 1-pyrazolyl, 1-triazolyl, 1-tetrazolyl, 1-piperazinyl, 1-homopiperazinyl, 1, 2- Called dihydropyridazin-1-yl, 1,2-dihydropyrimidin-1-yl, perhydropyrimidin-1-yl and 1,4-diazacycloheptan-1-yl; examples of cyclic amino groups with saturated
• R 1 for hydrogen, straight-chain or branched C 1-6 alkyl, in particular methyl, ethyl, propyl, isopropyl, sec-butyl, tert-butyl, C 3-6 t-cycloalkyl, in particular cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, aryl -C 1-2 alkyl, especially phenylmethyl or for hetaryl C 1-2 alkyl, especially
• R 1 and R 2 together with the atoms to which they are attached represent a 5- or 6-membered ring which can optionally be interrupted by sulfur and is optionally substituted by hydroxy,
• R 2 represents hydrogen, straight-chain or branched alkyl having up to 6 carbon atoms, in particular methyl, ethyl, propyl, isopropyl, sec-butyl, tert-butyl, hydroxy-C 1-2 -alkyl, in particular hydroxymethyl, 1-hydroxyethyl, C 1 -4- alkanoyloxy-C 1-4 -alkyl, especially acetoxymethyl, 1-acetoxyethyl, C 1 -4 -alkoxy-C 1-4 -alkyl, especially methoxymethyl, 1-methoxyethyl, aryl-C 1-4 -alkoxy- C 1-4 alkyl, especially benzyloxymethyl, 1-benzyloxym ethyl, mercapto-C 1 -4 alkyl, especially mercaptomethyl, C 1-4 alkylthio-C 1-4 alkyl, especially methyl sulfinylmethyl, C 1 -4 - Alkyl s
• C 1-4 alkylamino especially methylamino, C 1 -4 -di-alkylamino, especially dimethylamino, C 3-6 -cycloalkylamino, especially pyrrolidino, piperidino, C 3-6 -cycloalkylthioamino, especially thiomorpholino and dioxothiomorpholino, C 3 -6 -cycloalkyldiamino, in particular N-methylpiperazino, can be substituted, and R 3 and R 4 represent hydrogen,
• R 5 represents hydrogen, straight-chain or branched alkyl having up to 6 carbon atoms, in particular methyl, ethyl, propyl, isopropyl, sec-butyl, tert-butyl, hydroxy-C 1-2 -alkyl, in particular hydroxymethyl, 1-hydroxyethyl, C 1 -4- alkanoyloxy-C 1-4 alkyl, especially acetoxymethyl.
• C 1-4 -alkylthio-C 1-4 -alkyl in particular methylsulfinylmethyl, C 1 -4 -alkyl-sulfonyl-C 1 -4 -alkyl, in particular methylsulfonylethyl, carboxy-C 1-4 -alkyl, in particular carboxymethyl, carboxyethyl, C 1 -4 -alkoxycarbonyl-C 1 -4 - alkyl, in particular methoxycarbonylmethyl, ethoxycarbonylmethyl, aryl- C 1 -4 -alkoxycarbonyl-C 1 -4 -alkyl, in particular benzyloxycarbonylmethyl, carbamoyl-C 1 -4 - alkyl, in particular carbamoylmethyl, carbamoylethyl, amino-C 1 -4 alkyl, in particular aminopropyl, aminobutyl, C1 -4 - alkylamino-C 1 -4 alkyl,
• Carbon atoms especially vinyl, 2-propenyl, 2-butenyl, 1-methyl-2-propenyl, C 3-6 cycloalkyl-C 1-2 alkyl, especially cyclopropylmethyl, cyclobutylmethyl, cyclohexylmethyl, hetaryl-C 1-2 alkyl , in particular benzo [b] thien-1-yl-methyl, benzo [b] thien-3-yl, pyrid-2-yl-methyl, pyrid-3-yl-methyl, pyrid-4-yl-methyl, fur -2-yl-methyl, fur-3-yl-methyl, thien-2-yl-methyl, thien-3-yl-methyl, indol-3-yl-methyl, N-methyl-indol-3 -yl-methyl , Imidazol-4-yl-methyl, N-methylimidazol-4-yl-methyl, aryl-C 1-2 -alkyl, in particular
• R 7 represents hydrogen or C 1-4 alkyl, in particular methyl or ethyl, and straight-chain or branched C 1-4 alkyl, in particular methyl, ethyl, propyl, isopropyl, sec-butyl, tert-butyl, C 1- 4 -haloalkyl, in particular
• Haloalkyl in particular trifluoromethyl, difluoromethyl or trichloromethyl, C 1 -4 alkoxy, particularly methoxy, C 1-4 haloalkoxy, in particular trifluoromethoxy, difluoromethoxy, C 1 -4 - alkylthio, in particular methylthio, C1-4 -halogenoalkylthio, in particular trifluoromethylthio, , Nitro, amino, C 1 -4 -alkylamino, in particular methylamino, C 1 -4 -dialkylamino, in particular dimethylamino, or optionally for a radical from the group G 2 and G 3 ,
• Y represents oxygen, sulfur or -NR 9 ,
• R 8 is a cyclic amino group linked via a nitrogen atom, in particular 1-azetidinyl, pyrrolidino, 2-pyrrolin-1-yl, 1-pyrrolyl, piperidino, 1,4-dihydropyridin-1-yl , 1-imidazolidinyl, 1-imidazolyl, 1-pyrazolyl, 1-triazolyl, 1-tetrazolyl, 1-piperazinyl, 1-homopiperazinyl, 1,2-dihydro-pyridazin-1-yl, 1,2-dihydropyrimidin-1-yl , Perhydropyrimidin-1-yl, 1,4-diazacyclo-heptan-1-yl, thiazolidin-3-yl, isothiazolin-2-yl, morpholino, thiomorpholino, dioxothiomorpholino, which may be replaced by residues from the series halogen, in particular fluorine
• R 8 and R 9 independently of one another are hydrogen, straight-chain or branched C 1 -4 -alkyl, in particular methyl, ethyl, propyl, isopropyl, sec-butyl, tert-butyl, C 2-4 -alkenyl, in particular vinyl, 2-propenyl , 1-methyl-2-propenyl and 2-butenyl, C 2-4 alkynyl, especially ethynyl, 2-propynyl and 2-butynyl, C 3-6 cycloalkyl, especially cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl, C 3- 6- cycloalkyl-C 1-2 -alkyl, in particular cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl and cyclohexylmethyl, hetaryl, in particular pyridyl and thiazolyl, hetaryl-C
• C 1-4 - alkyl carbonyl in particular methylcarbonyl
• C 1-4 - alkoxycarbonyl in particular methoxycarbonyl
• Alkyl in particular aminomethyl, aminoethyl, C 1-4 -monoalkylamino-C 1-4 -alkyl, in particular methylaminomethyl, methylaminoethyl, C 1-4 -dialkylamino-C 1 -4 -alkyl, in particular dimethylaminomethyl, dimethylaminoethyl, amino, hydroxy, C. 1 -4 -alkoxy, in particular methoxy, C 1-4 -alkylcarbonyl, in particular methylcarbonyl, C 1 -4 -alkoxycarbonyl, in particular methoxycarbonyl, halogen, in particular fluorine, chlorine, bromine or iodine, are substituted,
• R 10 represents hydrogen or C 1 -4 alkyl, in particular methyl, ethyl, propyl, isopropyl, sec-butyl, tert-butyl, and
• R 11 for hydrogen, straight-chain or branched C 1-6 alkyl, in particular methyl, ethyl, propyl, isopropyl, sec-butyl, tert-butyl, C 2-6 alkenyl, in particular vinyl, 2-propenyl, 1-methyl 2-propenyl and 2-butenyl, C 2-6 alkynyl, in particular ethynyl, 2-propynyl and 2-butynyl, C 3-6 cycloalkyl, in particular cyclopropyl, cyclobutyl,
• Pentyl 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1,2-dimethylpropyl, 1,1-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, hexyl, 1-methylpentyl, C 1 -4 -alkylcarbonyl, in particular Methylcarbonyl, ethylcarbonyl, n-propylcarbonyl, isopropylcarbonyl, n-butylcarbonyl, isobutylcarbonyl, sec-butyl carbonyl, tert-butyl carbonyl, pentyl carbonyl, 1-methylbutylcarbonyl, 2-methylbutylcarbonyl, C j .
• 6- alkylsulfonyl especially methyl sulfonyl, ethylsulfonyl, n-propylsulfonyl, isopropyl sulfonyl, n-butylsulfonyl, isobutylsulfonyl, sec-butylsulfonyl, C 2-6 alkenyl, especially vinyl, 2-propenyl, 2-butenyl, 3-butenyl, 1 -Methyl-2-propenyl, 2-pentenyl, 3-pentenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1,1-dimethyl-2-propenyl, 1 , 2-dimethyl-2-propenyl, 1-ethyl-2-propenyl, 2-hexenyl, 1,2-dimethyl-3-butenyl, 2,3-dimethyl-2-butenyl, 1-ethyl
• Butyloxy, nitro, amino, C 1 -4 alkylamino, especially methylamino, C 1-4 dialkylamino, especially dimethylamino, C 3 -C 6 cycloalkylamino, especially piperidino and morpholino, are substituted, or R 12 and R 13 together with the adjacent N atom for a carbocyclic 5-, 6-, 7- or 8-membered ring system or for a 7 to 10-membered bicyclic ring system, which may also be replaced by oxygen, sulfur, sulfoxyl, sulfonyl, carbonyl, -NO -, -N , -NR 11 - or can be interrupted by quaternized nitrogen and optionally by aryl, in particular phenyl, C 1-4 -alkyl, in particular methyl, hydoxy-C 1-4 -alkyl, in particular hydroxymethyl, amino-C 1-4 -alkyl, in particular aminomethyl, aminoethyl, C
• R 14 represents hydrogen, straight-chain or branched C 1-6 alkyl, in particular methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, pentyl, 1-methylbutyl, 2-methylbutyl, 3- methylbutyl, 1, 2-dimethylpropyl, 1, 1 -dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, hexyl, 1-methylpentyl, C 3-6 - cycloalkyl, especially cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, which otherwise are substituted,
• R 15 and R 16 independently of one another are hydrogen, straight-chain or branched C 1-6 -alkyl, in particular methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1,2-dimethylpropyl, 1,1-dimethylpropyl, 2,2-dimethylpropyl, 1-ethyl propyl, hexyl, 1-methylpentyl, C 1-6 alkylcarbonyl, especially methylcarbonyl, ethylcarbonyl, n -Propylcarbonyl, isopropylcarbonyl, n-butylcarbonyl, isobutylcarbonyl, sec-butylcarbonyl, tert-butylcarbonyl, pentylcarbonyl, 1-methylbutylcarbonyl
• R 15 and R 16 together with the adjacent NO group represent a carbocycli see 5-, 6- or 7-membered ring, with the proviso that
• R 1 represents hydrogen and methyl and R 5 represents hydrogen and represents carboxy
• G 2 represents tert-butyloxy, benzyloxy and 4-nitro-benzyloxy
• B represents radicals other than tert-butyloxy, benzyloxy and 4-nitro-benzyloxy, and the optical isomers and racemates thereof.
• R 1 represents hydrogen, straight-chain or branched C 1-4 alkyl, in particular methyl, ethyl, C 3-6 cycloalkyl, in particular cyclopropyl
• R 2 represents hydrogen, straight-chain or branched C 1-4 alkyl in particular
• R 3 and R 4 represent hydrogen
• R 5 is hydrogen, straight-chain or branched C 1-4 alkyl, in particular methyl, ethyl, propyl, isopropyl, sec-butyl, hetaryl-C 1 -2 -alkyl, in particular pyrid-2-yl-methyl, pyrid-3- yl-methyl, pyrid-4-yl-methyl,
• R 6 C 1 -4 -haloalkylcarbonyl in particular trifluoromethylcarbonyl, trichloromethylcarbonyl, alkyl-C 1-4 -sulfonyl, in particular methylsulfonyl, ethylsulfonyl, nitro or cyano, and
• Y represents oxygen or -NR 9 ,
• R 8 is a cyclic amino group linked via a nitrogen atom, in particular pyrrolidino, 2-pyrrolin-1-yl, 1-pyrrolyl, piperidino, 1,4-dihydropyridin-1-yl, 1-piperazinyl , 1-homopiperazinyl, morpholino, thiomorpholino, dioxothiomorpholino, which is optionally substituted by radicals from the series halogen, especially fluorine, chlorine, bromine or iodine, C 1-4 - alkyl alkyl, in particular methyl, hydoxy-C1-4, especially hydroxymethyl , Amino-C 1-4 -alkyl, in particular aminomethyl, aminoethyl, C 1-4 -monoalkylamino-C 1 -4 -alkyl, in particular methylaminomethyl, methylaminoethyl, C 1-4 -dialkylamino-C 1 -4 -al
• Methoxycarbonyl may be substituted means
• R 8 and R 9 independently of one another for straight-chain or branched C 1-4 alkyl, in particular methyl, ethyl, propyl, isopropyl, sec-butyl, C 2-4 alkenyl, in particular vinyl, 2-propenyl, 1-methyl -2 propenyl, C 2-4 alkynyl, especially ethynyl, 2-propynyl, C 3-6 Cycloalkyl, in particular cyclopropyl, hetaryl-C 1-2 alkyl, in particular pyridylmethyl and thiazolylmethyl, which may be replaced by residues from the halogen, in particular fluorine, chlorine, bromine or iodine, C 1-4 -alkyl, in particular methyl, hydoxy-C 1-4 alkyl, especially hydroxymethyl, aminoC 1-4 alkyl, especially
• R 8 and R 9 together with the adjacent N atom for a carbocyclic 5-, 6- or 7-membered ring system which may also be replaced by oxygen, sulfur, sulfoxyl, sulfonyl, carbonyl,
• C 1-4 -alkyl in particular methyl, hydroxy-C 1-4 -alkyl, in particular hydroxymethyl, amino-C 1-4 -alkyl, in particular Aminomethyl, aminoethyl, C 1 -4 -monoalkylamino- C 1 -4 -alkyl, especially methylaminomethyl, methylaminoethyl, C 1-4 -dialkylamino-C 1-4 -alkyl, especially dimethylaminomethyl, dimethylaminoethyl, amino, hydroxy, C 1-4 Alkoxy, in particular methoxy, C 1-4 alkylcarbonyl, in particular methylcarbonyl, C 1-4 alkoxycarbonyl, in particular methoxycarbonyl, halogen, in particular fluorine, chlorine, bromine or iodine, are substituted,
• R 10 represents hydrogen or C 1 -4 alkyl, in particular methyl
• R 11 is hydrogen, straight-chain or branched C 1-6 alkyl, in particular methyl, ethyl, C 2-6 alkenyl, in particular vinyl, C 3-6 cycloalkyl, in particular cyclopropyl, C 1 -4 alkylcarbonyl, in particular methylcarbonyl, C 3-6 cycloalkylcarbonyl, in particular
• 3 8- cycloalkyloxy especially cyclopropyloxy, cyclohexyloxy, C 3-7 -cycloalkyl-C 1-2 alkyloxy, especially cyclopropylmethoxy, cyclohexylmethoxy, aryloxy-, especially phenoxy, aryl-C 1-2 -alkyloxy, especially benzyloxy, hetaryloxy, especially pyridyloxy , Hetaryl-C 1-2 alkyloxy, especially pyridylmethyl and thiazolylmehyl, which may be replaced by radicals from the halogen, especially fluorine, chlorine, bromine or iodine, hydroxy, C 1 -4 - alkyl, especially methyl, C 1 -4 - Haloalkyl, especially trifluoromethyl, trichloromethyl, amino, hydroxy, C 1-4 alkoxy, especially methoxy, C 1-2 alkylenedioxy, especially methylenedi
• Hydoxy-C 1-4 -alkyl in particular hydroxymethyl, amino-C 1-4 -alkyl, in particular aminomethyl, aminoethyl, C 1 -4 -monoalkylamino-C 1-4 -alkyl, in particular methylaminomethyl, methylaminoethyl, C 1-4 - Dialkylamino-C 1-4 alkyl, especially dimethylaminoethyl, C 3-6 cycloalkylamino, especially pyrrolidino, piperidino or
• Morpholino, amino, hydroxy, C 1-4 alkoxy, in particular methoxy, C 1 -4 alkylcarbonyl, in particular methylcarbonyl, C 1 -4 alkoxycarbonyl, in particular methoxycarbonyl, are substituted, or a radical from the groups G 4 , G 5 , G 6 , G 7 and G 8
• n can mean the numbers 0, 1, 2 or 3,
• R 14 represents hydrogen, straight-chain or branched C 1-6 alkyl, in particular methyl, ethyl, sec-butyl, C 3-6 cycloalkyl, in particular cyclopropyl
• R 15 and R 16 independently of one another are hydrogen, straight-chain or branched C 1-6 -alkyl, in particular methyl, ethyl, sec-butyl, C 1-6 -alkylcarbonyl, in particular methylcarbonyl, sec-butylcarbonyl, C 2-6 -alkenyl, in particular 2-propenyl, 1-methyl-2-propenyl, 1,1-dimethyl-2-propenyl, C 2-6 alkynyl, in particular 2-propynyl, C 3-6 cycloalkyl, in particular
• R 15 and R 16 together with the adjacent NO group represent a carbocyclic 5-, 6- or 7-membered ring, with the proviso that R 1 is hydrogen and methyl and R 5 is hydrogen and
• G 2 represents tert-butyloxy, benzyloxy and 4-nitro-benzyloxy
• B represents radicals other than tert-butyloxy, benzyloxy and 4-nitrobenzyloxy, and the optical isomers and racemates thereof.
• R 1 represents straight-chain or branched C 1-4 alkyl, in particular methyl
• R 2 represents straight-chain or branched C 1-4 alkyl, in particular methyl or ethyl,
• R 3 and R 4 represent hydrogen
• R 3 is hydrogen, represents straight-chain or branched C 1-4 alkyl, in particular methyl or ethyl,
• Y represents oxygen or -NR 9
• R 8 and R 9 independently of one another for straight-chain or branched C 1 -4 alkyl, in particular methyl, ethyl, propyl, isopropyl, sec-butyl, C 2-4 alkenyl, in particular vinyl, 2-propenyl, 1-methyl -2 -propenyl and C 2-4 - alkynyl, in particular ethynyl, 2-propynyl, C 3-6 -cycloalkyl, in particular cyclopropyl, hetaryl-C 1-2 -alkyl, in particular 2-chloro-pyrid-5-yl-methyl and 2 -Chlorthiazol-5-yl-methyl, stand, or
• R 8 and R 9 together with the adjacent N atom for a carbocyclic 5-, 6- or 7-membered ring system which may also be replaced by oxygen,
• Sulfur, sulfonyl, carbonyl, -N , -NR 11 - or can be interrupted by quaternized nitrogen and optionally by C 1-4 -alkyl, in particular methyl, C 1 -4 -dialkylamino-C 1-4 -alkyl, in particular dimethylaminomethyl , Hydroxy, C 1-4 -alkoxycarbonyl, particularly preferably for methoxycarbonyl, is substituted, in particular pyrrolidino, 3-oxopyrrolidino, morpholino, 2,6-dimethylmorpholino, thiomorpholino, dioxothiomorpholino,
• R 10 represents hydrogen or C 1-4 alkyl, in particular methyl
• R 11 straight-chain or branched C 1 . 6 - alkyl, especially methyl, C 2-6 - alkenyl, especially vinyl, C 3-6 cycloalkyl, especially cyclopropyl, C 1-4 alkylcarbonyl, especially methylcarbonyl, C 3-6 cycloalkylcarbonyl, especially cyclopropylcarbonyl, cyclohexylcarbonyl, C 1-4 -alkoxycarbonyl, especially methoxycarbonyl, hydroxy-C 1-4 -alkyl, especially hydroxyethyl, hydroxysulfonylethyl, C 1 -4 -alkylamino, especially ethylamino, C 1 -4 -dialkylamino-C 1-4 -alkyl, especially dimethylaminoethyl C 3-7 -cycloalkylamino-C 1-4 -alkyl, in particular N-morpholinoethyl, N-piperidinoethy
• C 1-6 alkoxy in particular methoxy, ethoxy, n-propoxy, sec-butoxy and tert-butoxy, C 2-6 alkenyloxy, 2-propenyloxy, 1,1-dimethyl-2-propenyloxy, C 2-6 alkynyloxy, in particular
• R 12 and R 13 independently of one another represent hydrogen, straight-chain or branched C 1 .
• n can mean the numbers 0, 1 or 2
• R 14 represents hydrogen, straight-chain or branched C 1-6 alkyl, in particular methyl
• R 15 and R 16 independently of one another are hydrogen, straight-chain or branched C 1 -6- alkyl, in particular methyl, C 1 -6- alkylcarbonyl, in particular
• Cyclopropyl is, with the proviso for the case that R 1 is hydrogen and methyl and
• R 5 represents hydrogen
• G 2 represents tert-butyloxy, benzyloxy and 4-nitro-benzyloxy
• B represents radicals other than tert-butyloxy, benzyloxy and 4-nitrobenzyloxy, and the optical isomers and racemates thereof.
• the compound of general formula (I) to be used according to the invention and their salts also contain one or more centers of chirality and can thus be present in pure stereoisomers or in the form of various enantiomer and diastereoisomer mixtures which, if necessary, can be separated in a manner known per se.
• the invention therefore relates both to the pure enantiomers and diastereomers and to their mixtures for controlling endoparasites, particularly in the field of medicine and veterinary medicine.
• optically active, stereoisomeric forms of the compounds of the general formula (I) and their salts are preferably used according to the invention.
• Suitable non-toxic salts, ie salts with different bases and salts with added acids can be mentioned as suitable salts of the compounds of the general formula (I).
• Formula (II) provides a general definition of the N-terminally acylated N-alkylamino acids required as starting materials for carrying out process 3a according to the invention.
• R 1 , R 2 , R 3 , G, Q and X preferably represent those radicals which have already been mentioned as preferred for these substituents in connection with the description of the substances of the general formula (II) according to the invention.
• N-acylated N-alkylamino acids of the general formula (II) used as starting materials are known (see, for example: N-methylamino acids:
• the carboxylic acid derivatives also to be used as starting materials for carrying out process 3a according to the invention are generally characterized by
• R 4 , R 5 , B and Z have the meaning which have already been mentioned as preferred for these substituents in connection with the description of the substances of the general formula (Ia) according to the invention.
• the compounds of the formula (III) are generally known compounds of organic chemistry or can be obtained by methods known from the literature (for example: 2-hydroxycarboxylic acid derivatives: see Houben-Weyl, Methods of Organic Chemistry, Volume VIII; 2-halocarboxylic acid derivatives: SM Birnbaum et al. J. Amer. Chem. Soc. 76 (1954) p. 6054, CS Rondestvedt, Jr. et al. Org.
• the reaction of the N-acylated N-alkylamino acids (II) with 2-hydroxycarboxylic acid derivatives (III) is preferably carried out in the presence of coupling reagents and in the presence of a basic reaction auxiliary using diluents.
• Coupling reagents for carrying out method 3a are all those which are suitable for producing an amide bond (cf., for example: Houben-Weyl, Methods of Organic Chemistry, Volume 15/2; Bodanszky et al., Peptide Synthesis 2nd ed. (Wiley & Sons , New York 1976) or Gross, Meienhofer, The Peptides: Analysis
• phosphonium reagents such as bis (2-oxo-3-oxazolidinyl) -phosphonium chloride (BOP-Cl), benzotriazol-1-yl-oxy-tris (dimethylamino-phosphonium) hexafluorophosphate (BOP) and phosphonic acid ester reagents, such as Diethyl cyanophosphonate (DEPC) or diphenylphosphoryl azide (DPPA)
• DEPC Diethyl cyanophosphonate
• DPPA diphenylphosphoryl azide
• Examples include the hydroxides, oxides and carbonates of lithium, sodium, potassium, magnesium, calcium and barium, as well as further basic compounds such as amidine bases or guanidine bases such as 7-methyl-1,5,7-triazabicyclo (4.4.0) dec- 5-s (MTBD); Diazabicyclo (4.3.0) nonen (DBN),
• Cyclohexyl-tetrabutylguanidine (CyTBG), cyclohexyltetramethylguanidine (CyTMG), N, N, N, N-tetramethyl-1,8-naphthalenediamine, pentamethylpiperidine, tertiary amines such as triethylamine, trimethylamine, tribenzylamine, triisopropylamine,
• Tributylamine tribenzylamine, tricyclohexylamine, triamylamine, trihexylamine,
• Tertiary amines in particular trialkylamines such as triethylamine, N, N-diisopropylethylamine, N-propyldiisopropylamine, N, N'-dimethylcyclohexylamine or N-methylmorpholine, are preferably used.
• diluents are advantageously used in an amount such that the reaction mixture remains readily stirrable throughout the process.
• Suitable diluents for carrying out process 3a according to the invention are all inert organic solvents.
• halogenated hydrocarbons in particular chlorinated hydrocarbons, such as tetrachlorethylene, tetrachloroethane, dichloropropane,
• esters such as methyl, ethyl, butyl, isobutyl acetate and dimethyl, dibutyl, ethylene carbonate;
• Amides such as hexamethylenephosphoric triamide, formamide, N-methylformamide, N, N-dimethylformamide, N, N-dipropylformamide, N, N-dibutylformamide, N-methyl-pyrrolidone, N-methyl-caprolactam, 1,3-dimethyl-3,4, 5,6-tetrahydro-2 (1H) pyrimidine, octyl pyrrolidone, octyl caprolactam, 1,3-dimethyl-2-imidazolinedione, N-formylpiperidine, N, N'-1,4-
• mixtures of the solvents and diluents mentioned can also be used in the process according to the invention.
• Preferred diluents are halogenated hydrocarbons, in particular chlorinated hydrocarbons, such as methylene chloride or 1,2-dichloroethane and
• Process 3a is generally carried out by combining compounds of the formula (II) in the presence of one of the stated coupling reagents and in the presence of one of the stated basic reaction auxiliaries of the general formula (III) in one of the specified diluents.
• the reaction time is 4 to 72 hours.
• the reaction takes place at temperatures between -10 ° C and + 120 ° C, preferably between -5 ° C and + 50 ° C, particularly preferably at 0 ° C to room temperature. It is operated under normal pressure.
• reaction solution is washed, the organic phase is separated off, dried and concentrated in vacuo.
• the products obtained can be purified in the usual way by recrystallization, vacuum distillation or column chromatography (cf. also the preparation examples).
• the didepsipeptides according to the invention can also be prepared by conventional methods, for example the one described by H.-G. Lerchen and H. Kunz (Tetrahedron Lett. 26 (43) (1985) pp. 5257-5260; 28 (17)
• N-methyl-L-alanyl-D-lactic acid methyl ester is used as compounds of the general formula (Ib) and trimethylallophanoyl chloride as compounds of the general formula (IV), the process can be carried out reproduce the following reaction scheme:
• Formula (Ib) provides a general definition of the N-terminally deblocked didepsipeptides required as starting materials for carrying out process 3b according to the invention.
• R 1 , R 2 , R 3 , R 4 , R 5 and B preferably represent those radicals which have already been mentioned as preferred for these substituents in connection with the description of the substances of the general formula (Ia) according to the invention.
• N-terminally deblocked didepsipeptides of the general formula (Ib) used as starting materials are known in some cases (cf. DE-OS 4,341,991, DE-OS 4,341,992, DE-OS 4,341,992) or can be prepared by the processes described therein can be obtained from N-terminally protected didepsipeptides.
• the compounds of formula (IV) are generally known compounds of organic chemistry or can be obtained by methods known from the literature
• the reaction of the compounds (Ib) with (IV) is preferably carried out in the presence of a basic reaction auxiliary using diluents.
• a basic reaction auxiliary using diluents.
• the inert, aprotic solvents mentioned in process 3a such as dioxane, acetonitrile or tetrahydrofuran, but also halogenated hydrocarbons, in particular chlorinated hydrocarbons, such as methylene chloride, are used as diluents for carrying out process 3b according to the invention.
• Basic reaction auxiliaries for carrying out process 3b according to the invention are all acid binders mentioned in process 3a, but preferably tertiary amines, in particular trialkylamines such as triethylamine, N, N-diisopropylethylamine, N-propyl-diisopropylamine, N, N'-dimethylcyclohexylamine or N- Find methylmorpholine.
• Process 3b is carried out using compounds of the general
• the reaction time is 4 to 72 hours.
• the reaction takes place at temperatures between -10 ° C and + 150 ° C, preferably between -5 ° C and + 80 ° C, particularly preferably at 0 ° C to room temperature. It is operated under normal pressure.
• 1.0 to 3.0 mol, preferably 1.0 to 1.5 mol, of acylating agent are generally employed per mol of N-alkylamino acid of the formula (Ib).
• the reaction solution is washed, the organic phase is separated off, dried and concentrated in vacuo.
• the products obtained can be purified in the usual way by recrystallization, vacuum distillation or column chromatography (cf. also the preparation examples).
• Formula (Ib) provides a general definition of the N-terminally deblocked didepsipeptides required as starting materials for carrying out process 3c according to the invention.
• R 1 , R 2 , R 3 , R 4 , R 5 and B preferably represent those radicals which have already been mentioned as preferred for these substituents in connection with the description of the substances of the general formula (Ia) according to the invention.
• N-terminally deblocked didepsipeptides of the general formula (Ib) used as starting materials are known in some cases (cf. DE-OS 4,341,991,
• DE-OS 4 341 992, DE-OS 4 341 992) or can be obtained from the N-terminally protected didepsipeptides by the processes described therein.
• the compounds also to be used as starting materials for carrying out process 3c according to the invention are generally defined by the formulas (V) and (VI).
• R 8 , Y, G 1 , X 1 and X have the meaning which have already been mentioned as preferred for this substituent in connection with the description of the substances of the general formula (Ia) according to the invention.
• the compounds of the formula (VI) are generally known compounds of organic chemistry, and some of them can. can be obtained commercially or by methods known from the literature (Houben-Weyl, Methods of Organic Chemistry, Volume E4).
• the reaction of the compounds (Ib) with (VI) by process 3c according to the invention is preferably carried out in the presence of diluents, if appropriate in the presence of a basic reaction auxiliary.
• diluents such as, for example, nitriles
• Acetonitrile, propionitrile, butyronitrile, especially acetonitrile, and ethers such as ethyl propyl ether, n-butyl ether, diethyl ether, dipropyl ether, diisopropyl ether, di-n-butyl ether, diisobutyl ether, diisoamyl ether, tetrahydrofuran, dioxane, especially terahydrofuran and dioxane, use.
• Process 3c can also be carried out in the presence of basic reaction auxiliaries.
• basic reaction auxiliaries for carrying out process 3c according to the invention are all acid binders mentioned in process 3a, but preferably tertiary amines, in particular trialkylamines such as triethylamine, N, N-diisopropylethylamine or N-methylmorpholine, and amidine bases or guanidine bases such as diazabicyclo- (4.3.0) nuns (DBN),
• Process 3c is carried out by combining compounds of the general formula (Ib) with equimolar amounts of a compound of the formula (VI) in one of the diluents given above, optionally in the presence of a basic reaction auxiliary.
• the reaction time is 1 to 72 hours.
• the reaction is carried out at temperatures between -50 ° C to + 200 ° C, preferably in a temperature range between -20 ° C and + 150 ° C, in particular in a temperature range between -10 ° C and + 120 ° C.
• it is possible to work under normal pressure but it is also possible to work at elevated or reduced pressure. It is preferred to work at normal pressure or at pressures up to 15 bar. At higher temperatures it is advantageous to work under increased pressure, possibly also above 15 bar.
• reaction mixture is worked up by generally customary methods (cf. also the preparation examples).
• N-terminally deblocked didepsipeptides of the formula (Ib) as amino compounds react with carbon dioxide and an alkylating agent in the presence of metal carbonates to give carbamates of the general formula (Ia).
• process 3d for the preparation of the new didepsipeptides (Ia) uses tert-butyl N-methyl-L-alanyl-D-lactic acid, carbon dioxide, potassium carbonate and butyl bromide as compounds of the general formula (IX) as compounds of the general formula (Ib), the process can be represented by the following reaction scheme:
• N-terminally deblocked didepsipeptides of the general formula (Ib) used as starting materials are known in some cases (cf. DE-OS 4,341,991, DE-OS 4,341,992, DE-OS 4,341,992) or can be described according to those described therein
• dry ice The usual commercial product, optionally also known as “dry ice”, can be used as carbon dioxide in the process according to the invention.
• the alkylating agents of the formula (IX) which are also to be used as starting materials for carrying out process 3d according to the invention are generally known compounds of organic chemistry.
• R 8 has the meaning that has already been mentioned as preferred for this substituent in connection with the description of the substances of the general formula (Ia) according to the invention, and shark has the meaning of an electron-withdrawing leaving group.
• Suitable leaving groups are e.g. B. Halogen such as fluorine, chlorine, bromine and iodine, sulfonate such as aryl and perfluoroalkyl sulfonate, monosubstituted diazo and monosubstituted nitrato, and additionally in J.
• one or more basic compounds of the elements lithium, sodium, magnesium, potassium, calcium, rubidium, strontium, cesium, barium and / or ammonium can be used as the base-reacting compounds.
• Suitable basic compounds are, for example, basic salts, oxides, hydrides and hydroxides.
• Examples include: lithium hydride, sodium hydride, potassium hydride, calcium hydride, lithium hydroxide, sodium hydroxide, potassium hydroxide, rubidium hydroxide, magnesium hydroxide, calcium hydroxide, strontium hydroxide, barium hydroxide, lithium oxide, sodium peroxide, potassium oxide, potassium peroxide, calcium oxide, barium oxide, magnesium oxide, lithium carbonate, strontium hydrogen carbonate, lithium carbonate, lithium carbonate, lithium carbonate, lithium carbonate Rubidium bicarbonate, cesium bicarbonate, cesium carbonate, lithium cyanide, sodium cyanide, potassium cyanide, rubidium cyanide, ammonium bicarbonate, cesium carbonate, ammonium carbamate, potassium sulfide, potassium hydrogen sulfide, sodium sulfide, sodium hydrogen sulfide and / or their naturally occurring or synthetically, or for example, magnesium and / or synthetically obtainable or magnesium compounds, magnesium and / or synthetically obtainable, or the magnesium and / or synthetic
• alkali carbonates and / or hydrogen carbonates are preferred, very particularly preferably cesium carbonate or potassium carbonate.
• the basic reacting compounds can be used in anhydrous form or, in the case of salts which crystallize with water of hydration, also in hydrated form.
• anhydrous compounds are preferably used.
• amides such as hexamethylenephosphoric triamide, N, N-dimethylformamide, N, N-dipropylformamide, N, N-dibutylformamide, N-methyl-pyrrolidone or N-methyl-caprolactam, in particular N, N-dialkylformamides, such as N, N-dimethylformamide, and sulfoxides such as Dimethyl sulfoxide, tetramethylene sulfoxide, dipropyl sulfoxide, benzyl methyl sulfoxide, diisobutyl sulfoxide, dibutyl sulfoxide, diisoamyl sulfoxide, especially dimethyl sulfoxide, use.
• amides such as hexamethylenephosphoric triamide, N, N-dimethylformamide, N, N-dipropylformamide, N, N-dibutylformamide, N-methyl-pyrrolidone or N-methyl-cap
• method 3d can also be carried out in the presence of basic reaction auxiliaries, i.e. in the presence of further bases, for example in an amount of less than 0.5 mol, based on the base used.
• Such basic reaction auxiliaries for carrying out process 3b according to the invention are all acid binders mentioned in process 3a, but preferably tertiary amines, in particular trialkylamines such as triethylamine, N, N-diisopropylethylamine or N-methylmorpholine, and amidine bases or guanidine bases such as 7-methyl-1,5 , 7-triazabicyclo (4.4.0) dec-5-ene (MTBD); Diazabicyclo- (4.3.0) nonene (DBN), diazabicyclo (2.2.2) octane (DABCO), 1,8-diaza-bicyclo (5.4.0) undecene (DBU) cyclohexyltetrabutylguanidine (CyTBG), cyclohexyltetramethylguanidine (CyTMG) , Cyclohexyltetrabutylguanidin, N, N, N, N-tetramethyl-1,
• Process 3d is carried out by using compounds of the general formula (Ib) in the presence of carbon dioxide, a 2 to 3-fold excess of alkali metal carbonate of the formula (VII) and an alkylating agent of the formula
• Formula (Ie) provides a general definition of the N-terminally acylated didepsipeptides required as starting materials for carrying out process 3e according to the invention.
• R 1, R 2, R 3, R 4, R 5, G, W, X and B preferably represent those radicals which have as preferred in connection with the description of the substances of the general formula (Ia) according to the invention for these substituents are called.
• N-terminally acylated didepsipeptides of the general formula (Ib) used as starting materials are known in some cases (cf. DE-OS 4,341,991, DE-OS 4,341,992, DE-OS 4,341,992) can be obtained by the processes described therein are or can be represented by the method 3b according to the invention shown further above.
• nucleophilic agents of the formula (X) which are also to be used as starting materials for carrying out process 3e according to the invention are generally known compounds of organic chemistry.
• R 8 and Y have the meaning which have already been mentioned as preferred in connection with the description of the substances of the general formula (Ia) according to the invention.
• Process 3e is carried out by reacting compounds of the general formula (Ie) in the presence of a nucleophilic agent of the formula (X) in one of the diluents given above.
• the reaction time is 4 to 72 hours.
• the reaction takes place at temperatures between + 10 ° C and + 200 ° C, preferably between + 20 ° C and + 150 ° C, particularly preferably at
• Formula (Id) provides a general definition of the C-terminally deblocked didepsipeptides required as starting materials for carrying out process 3e according to the invention.
• R 1 , R 2 , R 3 , R 4 , R 5 , G, X and Q preferably represent those radicals which are already in connection with the description Exercise of the substances of the general formula (Ia) according to the invention can be mentioned as preferred for these substituents.
• the C-terminally deblocked didepsipeptides of the general formula (Id) used as starting materials are known in some cases (cf. DE-OS 4,341,991, DE-OS 4,341,992, DE-OS 4,341,992) or can be prepared by the processes described therein be preserved.
• the C-terminally deblocked didepsipeptides (Id) used as starting materials can be prepared using customary methods of C-terminal deblocking such as acidolysis, for example in the case of a tert-butyl ester, or catalytic hydrogenation, for example in the case of a benzyl ester.
• Formula (XI) generally defines the nucleophiles to be used as starting materials for carrying out process 3e according to the invention.
• the compounds of formula (XI) are generally known compounds of organic chemistry. can be obtained commercially or by methods known from the literature.
• reaction of the C-terminally deblocked didepsipeptides of the formula (Id) with compounds of the formula (XI) is preferably carried out in the presence of Kupp tion reagents and in the presence of a basic reaction auxiliary using diluents.
• Coupling reagents for carrying out process 3f are all coupling reagents which are suitable for producing an amide bond and have already been used in process 3 a mentioned above.
• phosphonium reagents such as bis (2-oxo-3-oxazolidinyl) -phosphonium acid chloride (BOP-Cl), benzotri azole-1 -yl-oxytris (dimethylaminophosphonium) hexafluorophosphate (BOP) and phosphonic acid ester reagents, such as diethyl cyanophosphonate (DE), is preferred ) or diphenylphosphoryl azide (DPPA).
• BOP-Cl bis (2-oxo-3-oxazolidinyl) -phosphonium acid chloride
• BOP benzotri azole-1 -yl-oxytris (dimethylaminophosphonium) hexafluorophosphate
• phosphonic acid ester reagents such as diethyl cyanophosphonate (DE), is preferred ) or diphenylphosphoryl azide (DPPA).
• All of the acid binders suitable for process 3a can also be used as basic reaction auxiliaries for carrying out process 3f according to the invention.
• Tertiary amines in particular trialkylamines such as triethylamine, N, N-diisopropylethylamine, N-propyldiisopropylamine, N, N'-dimethyl-cyclohexylamine or N-methylmorpholine, are preferably suitable.
• the solvents mentioned in method 3a such as, for. B. halogenated hydrocarbons, especially chlorinated hydrocarbons, such as methylene chloride or 1,2-dichloroethane and mixtures of these with other diluents mentioned, use.
• halogenated hydrocarbons especially chlorinated hydrocarbons, such as methylene chloride or 1,2-dichloroethane and mixtures of these with other diluents mentioned, use.
• Process 3j is generally carried out by reacting compounds of the formula (Id) in the presence of one of the stated coupling reagents and in the presence of one of the stated basic reaction auxiliaries with compounds of the general formula (XI) in one of the stated diluents.
• the reaction time is 4 to 72 hours.
• the reaction takes place at temperatures between -10 ° C and + 120 ° C, preferably between -5 ° C and + 50 ° C, particularly preferably at 0 ° C to room temperature. It is operated under normal pressure.
• 1.0 to 3.0 mol, preferably 1.0 to 1.5 mol, of coupling reagent are generally employed per mol of C-terminally deblocked didepsipeptide of the formula (Id).
• reaction solution is washed, the organic phase is separated off, dried and concentrated in vacuo.
• the products obtained can be purified in the usual way by recrystallization, vacuum distillation or column chromatography (cf. also the preparation examples).
• didepsipeptides can be obtained from the individual building blocks with both L and D configurations while maintaining, but also with inversion of the original configuration of the starting materials.
• inert solvents mean solvents which are inert under the respective reaction conditions but do not have to be inert under any reaction conditions.
• the active ingredients are suitable for combating pathogenic endoparasites, which occur in humans and in animal husbandry and animal breeding in useful, breeding, zoo, laboratory, experimental and hobby animals, with favorable warm-blooded toxicity. They are effective against all or individual stages of development of the pests and against resistant and normally sensitive species. By combating the pathogenic endoparasites, illness, deaths and reduced performance (e.g. in the production of meat, milk, wool, hides, eggs, honey, etc.) are to be reduced, so that the use of the active ingredients enables more economical and easier animal husbandry.
• Pathogenic endoparasites include cestodes, trematodes, nematodes, acantocephals, in particular:
• Cyclophyllidea for example: Mesocestoides spp., Anoplocephala spp., Paranoplocephala spp., Moniezia spp., 'Thysanosomsa spp., Thysaniezia spp., Avitellina spp., Stilesia spp., Cittotaenia spp., Andyella spp., Bertella spp ., Taenia spp., Echinococcus spp., Hydatigera spp., Davainea spp., Raillietina spp., Hy menolepis spp., Echinolepis spp., Echinocotyle spp., Diorchis spp., Dipylidium spp., Joyeuxiella spp., Diplopylidium spp ...
• Gigantobilharzia spp. Leucochloridium spp., Brachylaima spp., Echinostoma spp., Echinoparyphium spp., Echinochasmus spp., Hypoderaeum spp., Fasciola spp., Fasciolides spp., Fasciolopsis spp., Cyclocoelumlpp., Typhomistum spp ., Calicophoron spp., Cotylophoron spp., Gigantocotyle spp.,
• Fischoederius spp. Gastrothylacus spp., Notocotylus spp., Catatropis spp., Plagiorchis spp., Prosthogonimus spp., Dicrocoelium spp., Eurytrema spp., Troglotrema spp., Paragonimus spp., Collyriclyetppus., ., Clonorchis spp., Metorchis spp., Heterophyes spp., Metagonismus spp .. From the order of the Enoplida, for example: Trichuris spp., Capillaria spp., Trichomosoides spp., Trichinella spp ..
• Stronylus spp. Triodontophorus spp., Oesophagodontus spp., Trichonema spp., Gyalocephalus spp., Cylindropharynx spp., Poteriostomum spp., Cyclococercus spp., Cylicostephanus sppum, spp., Oesophag.
• Stephanurus spp. Ancylostoma spp., Uncinaria spp., Bunostomum spp., Globocephalus spp., Syngamus spp., Cyathostoma spp., Metastrongylus spp., Dictyocaulus spp., Muellerius spp., Protostrongylus spp., Neostr spp., Pneumostrongylus spp., Spicocaulus spp., Elaphostrongylus spp., Parelaphostrongylus spp., Crenosoma spp., Paracrenosoma spp., Angiostrongylus spp., Aelurostrongylus spp., Filaroides spp., Parongilarchides.
• Oxyurida From the order of Oxyurida, for example: Oxyuris spp., Enterobius spp., Passalurus spp ., Syphacia spp., Aspiculuris spp., H eterakis spp ..
• Ascaridia for example: Ascaris spp., Toxascaris spp., Toxocara spp., Parascaris spp., Anisakis spp., Ascaridia spp ..
• Livestock and breeding animals include mammals such as Cattle, horses, sheep, pigs, goats, camels, water buffalos, donkeys, rabbits, fallow deer, reindeer, fur animals such as Mink, chinchilla, raccoon, birds such as Chickens, geese, turkeys, ducks, fresh and salt water fish such as Trout, carp, eels, reptiles, insects such as Honey bee and silkworm.
• mammals such as Cattle, horses, sheep, pigs, goats, camels, water buffalos, donkeys, rabbits, fallow deer, reindeer, fur animals such as Mink, chinchilla, raccoon, birds such as Chickens, geese, turkeys, ducks, fresh and salt water fish such as Trout, carp, eels, reptiles, insects such as Honey bee and silkworm.
• Laboratory and experimental animals include mice, rats, guinea pigs, golden hamsters, dogs and cats.
• the pets include dogs and cats.
• the application can be prophylactic as well as therapeutic.
• the active ingredients are used directly or in the form of suitable preparations enterally, parenterally, dermally, nasally, by treating the environment or with the aid of shaped articles containing active ingredients, e.g. Strips, plates, ribbons, collars, ear tags, limb straps, marking devices.
• enteral application of the active ingredients takes place e.g. orally in the form of powder, tablets, capsules, pastes, drinkers, granules, orally applicable solutions,
• Suspensions and emulsions, boluses, medicated feed or drinking water takes place, for example, in the form of dipping (dipping), spraying (spraying) or pouring on (pour-on and spot-on).
• Parenteral use happens for example in the form of injection (intramuscular, subcutaneous, intravenous, intraperitoneal) or by implants.
• Suitable preparations are:
• Solutions such as solutions for injection, oral solutions, concentrates for oral administration after dilution, solutions for use on the skin or in body cavities, pour-on formulations, gels;
• Emulsions and suspensions for oral or dermal use and for injection are Emulsions and suspensions for oral or dermal use and for injection; semi-solid preparations;
• Solid preparations such as powders, premixes or concentrates, granules, pellets, tablets, boluses, capsules; Aerosols and inhalants, molded articles containing active ingredients.
• Solutions for injection are administered intravenously, intramuscularly and subcutaneously.
• Injection solutions are prepared by dissolving the active ingredient in a suitable solvent and possibly additives such as solubilizers, acids,
• Bases can be added.
• the solutions are sterile filtered and filled.
• solvents physiologically compatible solvents such as water, alcohols such as ethanol, butanol, benzyl alcohol, glycerol, propylene glycol, polyethylene glycols, N-methyl-pyrrolidone, and mixtures thereof.
• the active compounds can also be dissolved in physiologically tolerable vegetable or synthetic oils which are suitable for injection.
• solubilizers solvents which promote the dissolution of the active ingredient in the main solvent or prevent its precipitation.
• solvents which promote the dissolution of the active ingredient in the main solvent or prevent its precipitation.
• examples are polyvinyl pyrrolidone, polyoxyethylated castor oil, polyoxyethylated sorbitan esters.
• Preservatives are: benzyl alcohol, trichlorobutanol, p-hydroxybenzoic acid ester, n-butanol.
• Oral solutions are applied directly. Concentrates are used orally after previous dilution to the application concentration. Oral solutions and concentrates are prepared as described above for the injection solutions, whereby sterile work can be dispensed with.
• Thickeners are: inorganic thickeners such as bentonites, colloidal silica, aluminum monostearate, organic thickeners such as cellulose derivatives, polyvinyl alcohols and their copolymers, acrylates and methacrylates.
• Gels are applied to or spread on the skin or placed in body cavities. Gels are produced by adding enough thickening agent to solutions which have been prepared as described for the injection solutions to form a clear mass with an ointment-like consistency.
• the thickeners specified above are used as thickeners. Pour-on formulations are poured or sprayed onto limited areas of the skin, the active ingredient penetrating the skin and acting systemically.
• pour-on formulations are prepared by dissolving, suspending or emulsifying the active ingredient in suitable solvents or solvent mixtures that are compatible with the skin. If necessary, other auxiliaries such as dyes, absorption-promoting substances, antioxidants, light stabilizers and adhesives are added.
• solvents water, alkanols, glycols, polyethylene glycols, polypropylene glycols, glycerin, aromatic alcohols such as benzyl alcohol, phenylethanol, phenoxyethanol, esters such as ethyl acetate, butyl acetate, benzyl benzoate, ethers such as alkylene glycol alkyl ethers such as dipropylene glycol monomethyl ether, diethylene glycol, methyl butylene glycol, methyl butylene glycol, methyl butylene glycol ethyl ketone, aromatic and / or aliphatic hydrocarbons, vegetable or synthetic oils, DMF, dimethylacetamide, N-methylpyrrolidone, 2,2-dimethyl-4-oxy-methylene-1,3-dioxolane.
• aromatic alcohols such as benzyl alcohol, phenylethanol, phenoxyethanol
• esters such as ethyl acetate, butyl acetate
• Dyes are all dyes approved for use on animals, which can be dissolved or suspended.
• Absorbing substances are e.g. DMSO, spreading oils such as isopropyl myristate, dipropylene glycol pelargonate, silicone oils, fatty acid esters, triglycerides, fatty alcohols.
• Antioxidants are sulfites or metabisulfites such as potassium metabisulfite, ascorbic acid, butylated hydroxytoluene, butylated hydroxyanisole, tocopherol.
• Light stabilizers are e.g. Novantisol acid.
• Adhesives are e.g. Cellulose derivatives, starch derivatives, polyacrylates, natural polymers such as alginates, gelatin.
• Emulsions can be used orally, dermally or as injections.
• Emulsions are either water in oil or oil in water. They are produced by dissolving the active ingredient either in the hydrophobic or in the hydrophilic phase and homogenizing it with the solvent of the other phase with the aid of suitable emulsifiers and, if necessary, other auxiliary substances such as dyes, absorption-promoting substances, preservatives, antioxidants, light stabilizers, viscosity-increasing substances .
• suitable emulsifiers if necessary, other auxiliary substances such as dyes, absorption-promoting substances, preservatives, antioxidants, light stabilizers, viscosity-increasing substances .
• Vegetable oils such as sesame oil, almond oil, castor oil, synthetic triglycerides such as caprylic / capric acid biglyceride, triglyceride mixture with vegetable fatty acids of chain length C 8-12 or other specially selected natural fatty acids, partial glyceride mixtures of saturated or unsaturated fatty acids also containing hydroxyl groups, mono- and diglycerides 8 / C 10 fatty acids.
• Fatty acid esters such as ethyl stearate, di-n-butyryl adipate, hexyl laurate, dipropylene glycol pelargonate, esters of a branched fatty acid of medium chain length saturated fatty alcohols of chain length C 16 -C 18 , isopropyl myristate, isopropyl palmitate, caprylic / capric acid esters of saturated fatty alcohols of chain length C 12 -C 18 , isopropyl stearate, oleic acid olylester, oleic acid decyl ester, ethyl oleate, lactic acid ethyl ester, wax-like fatty acid ester, dibutylester fatty acid such as dibutyl acetate, such as artificial dibutyl acetate, such as artificial dibutyl acetate, such as artificial dibutyl ester, related ester mixtures, inter alia
• Fatty alcohols such as isotridecyl alcohol, 2-octyldodecanol, cetylstearyl alcohol, oleyl alcohol.
• Fatty acids such as Oleic acid and its mixtures.
• the following can be mentioned as the hydrophilic phase:
• Alcohols such as e.g. Propylene glycol, glycerin, sorbitol and their mixtures.
• nonionic surfactants e.g. polyoxyethylated castor oil, polyoxyethylated sorbitan monooleate, sorbitan monostearate, glycerol monostearate, polyoxyethyl stearate, alkylphenol polyglycol ether
• ampholytic surfactants such as di-Na-N-lauryl- ⁇ -iminodipropionate or lecithin
• anionic surfactants such as sodium lauryl sulfate, fatty alcohol ether sulfates, mono / dialkyl polyglycol ether orthophosphoric acid ester monoethynolamine salt.
• auxiliaries substances which increase viscosity and stabilize the emulsion, such as carboxymethyl cellulose, methyl cellulose and other cellulose and starch derivatives, polyacrylates, alginates, gelatin, gum arabic,
• Polyvinylpyrrolidone polyvinyl alcohol, copolymers of methyl vinyl ether and maleic anhydride, polyethylene glycols, waxes, colloidal silica or mixtures of the substances listed.
• Suspensions can be used orally, dermally or as an injection. They are produced by suspending the active ingredient in a carrier liquid, optionally with the addition of other auxiliaries such as wetting agents, dyes, absorption-promoting substances, preservatives, antioxidants, light stabilizers. All homogeneous solvents and solvent mixtures may be mentioned as carrier liquids.
• surfactants specified above may be mentioned as wetting agents (dispersants). Further additives mentioned are those mentioned above.
• Semi-solid preparations can be administered orally or dermally. They differ from the suspensions and emulsions described above only in their higher viscosity.
• the active ingredient is mixed with suitable carriers, if appropriate with the addition of auxiliaries, and brought into the desired shape.
• Inorganic and organic substances serve as such.
• Inorganic substances are e.g. Table salt, carbonates such as calcium carbonate, hydrogen carbonates, aluminum oxides, silicas, clays, precipitated or colloidal silicon dioxide, phosphates.
• Organic substances are e.g. Sugar, cellulose, food and feed such as milk powder, animal meal, cereal flour and meal, starches.
• Excipients are preservatives, antioxidants, dyes, which have already been listed above.
• auxiliaries are lubricants and lubricants such as Magnesium stearate, stearic acid, talc, bentonite, decay-promoting substances such as starch or cross-linked polyvinylpyrrolidone, binders such as e.g. Starch, gelatin or linear polyvinylpyrrolidone and dry binders such as microcrystalline cellulose.
• lubricants and lubricants such as Magnesium stearate, stearic acid, talc, bentonite, decay-promoting substances such as starch or cross-linked polyvinylpyrrolidone, binders such as e.g. Starch, gelatin or linear polyvinylpyrrolidone and dry binders such as microcrystalline cellulose.
• the active substances can also be present in the preparations as a mixture with synergists or with other active substances which act against pathogenic endoparasites lie.
• Such active ingredients are, for example, L-2,3,5,6-tetrahydro-6-phenylimidazothiazole, benzimidazole carbamates, praziquantel, pyrantel, febantel.
• Ready-to-use preparations contain the active ingredient in concentrations of 10 ppm to 20 percent by weight, preferably 0.1 to 10 percent by weight.
• Preparations which are diluted before use contain the active ingredient in concentrations of 0.5-90% by weight, preferably 5-50% by weight.
• Active ingredient administered orally and / or intravenously.
• the efficiency is determined by quantitatively counting the worm eggs excreted in the faeces before and after the treatment.
• a complete suspension of egg excretion after treatment means that the worms have been aborted or are so damaged that they no longer produce eggs (effective dose).
• the efficiency is determined by quantitatively counting the worm eggs excreted in the faeces before and after the treatment.
• a complete suspension of egg excretion after treatment means that the worms have been aborted or are so damaged that they no longer produce eggs (effective dose).
• N- 3.8 g (29.1 mmol) of N, N- are added to a solution of 2.0 g (1.6 mmol) of N-methyl -L-al-anyl -D-lactic acid methyl ester in 100 ml of methylene chloride at 0 ° C.
• Diisopropylethylamine (“Hünig's base”) and 2.1 g (12.7 mmol) of trimethylallophanoic acid chloride were added, the mixture was stirred at 0 ° C. for two hours and then at room temperature for about 18 hours.
• the reaction solution is shaken twice with water, the organic phase is separated off and, after drying over sodium sulfate, concentrated in vacuo.
• Dry hydrogen chloride gas is passed into a solution of 11.8 g (32.8 mmol) of N-methyl-N-trimethylallophanoyl-L-alanyl-D-lactic acid tert-butyl ester in 250 ml of absolute methylene chloride, cooled to 0 ° C., for 20 minutes. The mixture is then stirred for about 16 hours at room temperature and the entire reaction mixture is concentrated in vacuo.

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• 1995
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  • 1996-07-30 CA CA002228939A patent/CA2228939C/en not_active Expired - Lifetime
  • 1996-08-05 TW TW085109422A patent/TW492976B/zh not_active IP Right Cessation
  • 1996-08-08 ZA ZA9606749A patent/ZA966749B/xx unknown
  • 1996-08-09 AR ARP960103941A patent/AR003977A1/es not_active Application Discontinuation
• 1998
  • 1998-01-26 NO NO19980324A patent/NO311566B1/no not_active IP Right Cessation
  • 1998-01-28 BG BG102213A patent/BG64091B1/bg unknown
• 1999
  • 1999-05-05 HK HK99102025A patent/HK1017340A1/xx not_active IP Right Cessation
  • 1999-09-09 CN CN99118744A patent/CN1254596A/zh active Pending
• 2002
  • 2002-11-08 US US10/290,827 patent/US7772190B2/en not_active Expired - Fee Related
• 2010
  • 2010-05-10 JP JP2010108807A patent/JP2010222361A/ja not_active Withdrawn
• 2014
  • 2014-04-11 JP JP2014082229A patent/JP2014159449A/ja active Pending

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